Polyether polyols, polyol formulation containing them and their use in the production of hard polyurethane foams

- Bayer Aktiengesellschaft

Polyol formulations, containing polyether polyols possessing 40 to 80 wt % of tertiary amino groups and having an OH number of 300 to 500, preferably 350 to 420, obtainable by addition of exclusively propylene oxide to o-toluylenediamine, which contain cyclopentane and/or n- and/or i-pentane and/or hydrofluoro alkanes as blowing agent, are used for the manufacture of rigid polyurethane foams by reacting with organic polyisocyanates, optionally further compounds with at least two hydrogen atoms reactive to isocyanates, optionally in the presence of water, and further blowing agents known per se as well as conventional auxiliaries and additives.

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Description
BACKGROUND OF THE INVENTION

It is known to manufacture rigid PUR foams using readily volatile alkanes and hydro-fluoro alkanes as blowing agents. The range of polyols is generally restricted in this case due to the low solubility of the above-mentioned blowing agents in most commercially available polyols and polyol mixtures. There are admittedly some polyol types with good solubility; trimethylolpropane- and ethylenediamine-started polyethers can be mentioned in particular here. In the case of trimethylolpropane ethers the low functionality has a disadvantageous effect on the mould retention time (curing of the foams obtained), while with higher concentrations of ethylenediamine-started polyethers an excessively high inherent activity of the foam formulation is obtained.

DETAILED DESCRIPTION OF THE INVENTION

It has now been found that propylene oxide polyethers started on o-toluylenediamine on the one hand produce foams with satisfactory curing and on the other also possess a sufficiently low inherent activity, so that they can be added in sufficient concentration to the formulation as is necessary for the solubility of alkanes and hydro-fluoro alkanes.

It has also been shown that the o-toluene diamine-started polyethers are distinguished by a relatively low viscosity. In the papers on these polyethers it has furthermore been noted that relatively low-viscosity polyols can be obtained if the toluene diamine is first of all reacted with 3 mol of propylene oxide and then the desired OH number is set after the addition of an alkaline catalyst and further amounts of propylene oxide.

Polyols are thus obtained which are harmoniously attuned as regards solubility in the blowing agents to be used according to the invention, viscosity, inherent activity, influence on the flow properties of the rigid foams and a short mould retention time.

The invention provides polyether polyols possessing tert. amino groups and having an OH number of 300 to 500, preferably 350 to 420, obtainable by the addition of exclusively propylene oxide to o-toluene diamine,

a method for the manufacture of such polyether polyols, characterised in that o-toluene diamine is reacted first of all with 3 mol of propylene oxide and then after the addition of an alkali catalyst with further amounts of propylene oxide, until an OH number of 300 to 500, preferably 350 to 420, has been reached, and

a polyol formulation for rigid polyurethane foams, containing 40 to 80 wt % of the above-mentioned polyether polyols possessing tert. amino groups.

Preferred is

an above-mentioned polyol formulation, containing additionally sucrose polyether polyols with an OH number of 350 to 500 or containing additionally a mixture of sucrose polyether polyols with an OH number of 350 to 500 and phthalic acid ester polyols,

the above-mentioned polyol formulation, containing cyclopentane as blowing agent,

the above-mentioned polyol formulation, containing n- and/or i-pentane as blowing agent and

the above-mentioned polyol formulation, containing hydrofluoro alkanes such as 1,1,1,4,4,4-hexafluoro-butane and/or 1,1,1,3,3-pentafluoropropane as blowing agent.

The invention also relates to the use of the above-mentioned polyol formulations for the manufacture of rigid polyurethane foams by reacting with organic poly-isocyanates, optionally further compounds with at least two hydrogen atoms reactive to isocyanates, optionally in the presence of water, and further blowing agents known per se as well as conventional auxiliaries and additives.

Use is made according to the invention for the manufacture of rigid polyurethane foams of:

1. the above-mentioned polyether polyols possessing tert. amino groups and having an OH number of 300 to 500, preferably 350 to 420, obtainable by the addition of exclusively propylene oxide to o-toluene diamine. Their manufacture takes place e.g. in such a way that o-toluene diamine is reacted first of all with 3 mol of propylene oxide and then after the addition of an alkali catalyst with further amounts of propylene oxide, until an OH number of 300 to 500, preferably 350 to 420, has been reached. For the manufacture of rigid polyurethane foams they are generally used as a polyol formulation in which their content generally comes to 40 to 80 wt %.

The polyol formulations often contain additionally sucrose polyether polyols having an OH number from 350 to 500 and/or phthalic acid ester polyols.

The polyol formulations also contain cyclopentane and/or n- and/or i-pentane and/or hydrofluoroalkanes such as 1,1,1,4,4,4-hexafluorobutane and/or 1,1,1,3,3-pentafluoropropane as blowing agent. Also possible in the polyol formation is the use on a proportionate basis (up to 40 wt %) of other compounds with at least two hydrogen atoms reactive to isocyanates and a molecular weight of 62 to 10 000, preferably polyols such as the polyethers and polyesters known per se, as well as chain-extension and crosslinking agents (cf. DE-OS 2 832 253, pages 11 to 20).

Starting components for the manufacture of the rigid polyurethane foams are also

2. Aliphatic, cycloaliphatic, araliphatic, aromatic and heterocyclic polyisocyanates, such are described e.g. by W. Siefken in "Justus Liebigs Annalen der Chemie", 562, pages 75 to 136, for example those with the formula

Q(NCO).sub.n,

in which

n is 2 to 4, preferably 2 to 3, and

Q stands for an aliphatic hydrocarbon residue with 2 to 18, preferably 6 to 10, C-atoms, a cyclo-aliphatic hydrocarbon residue with 4 to 15, preferably 5 to 10, C-atoms, an aromatic hydrocarbon residue with 6 to 15, preferably 6 to 13, C-atoms or an araliphatic hydrocarbon residue with 8 to 15, preferably 8 to 13, C-atoms,

e.g. polyisocyanates such as are described in DE-OS 2 832 253, pages 10 to 11.

Particularly preferred are generally the technically easily accessible polyisocyanates, e.g. the 2,4- and 2,6-toluene diisocyanate and any mixtures of these isomers ("TDI"), polyphenylpolymethylene poly-isocyanates, such as are manufactured by aniline-formaldehyde condensation and subsequent phosgenation ("crude MDI") and carbodiimide groups, urethane groups, allophanate groups, isocyanurate groups, polyisocyanates containing biuret groups or urea groups ("modified polyisocyanates"), in particular polyisocyanates such as are derived from 2,4- and/or 2,6-toluene diisocyanate or from 4,4'- and/or 2,4'-diphenylmethanediisocyanate.

3. There are used as blowing agents n- and/or i-pentane and/or cyclopentane and/or hydrofluoroalkanes such as 1,1,1,4,4,4-hexafluorobutane and/or 1,1,1,3,3-pentafluoropropane.

Water and/or other readily volatile organic compounds can also be used as additional blowing agents.

4. Use is also made optionally of further auxiliaries and additives known per se, such as catalysts, emulsifiers, flame retardants and foam stabilizers.

Preferred as emulsifiers are those based on alkoxylated fatty acids and higher alcohols. There are considered as foam stabilizers in particular polyether siloxanes, in particular water-soluble representatives. These compounds are in general composed in such a way that a copolymer of ethylene oxide and propylene oxide is linked to a polydimethyl siloxane residue. Such foam stabilizers are described e.g. in U.S. Pat. Nos. 2,834,748, 2,917,480 and 3,629,308. The catalysts known per se from polyurethane chemistry such as tert.-amines and/or organometallic compounds can also be used.

Tricresyl phosphate, for example, may be mentioned as a flame retardant.

Reaction retardants, e.g. acid reacting substances such as hydrochloric acid or organic acid halides, also cell regulators of the kind known per se such as paraffins or fatty alcohols or dimethyl polysiloxanes as well as pigments or dyestuffs, also stabilizers against ageing and weathering influences, plasticizers and fungistatically and bacteriostatically acting substances as well as fillers such as barium sulphate, kieselguhr, carbon block or prepared chalks can also be used.

Further examples of surface-active additives and foam stabilizers as well as cell regulators, reaction retardants, stabilizers, flame-inhibiting substances, plasticizers, dyestuffs and fillers as well as fungistatically and bacteriostatically active substances which can be used optionally according to the invention, as well as details on method of use and mode of action of these additives, are described in "Kunststoff-Handbuch", Vol. VII, published by Vieweg and Hochtlen, Carl-Hanser-Verlag, Munich, 1966, e.g. on pages 103 to 113.

CARRYING OUT OF THE INVENTION

The reaction components are reacted according to the invention by the single-stage method known per se, the prepolymer method or the semi-prepolymer method, wherein use is often made of mechanical equipment, e.g. that which is described in U.S. Pat. No. 2,764,565. Details of processing equipment which is also considered according to the invention are described in "Kunststoff-Handbuch", Vol. VII, published by Vieweg and Hochtlen, Carl-Hanser-Verlag, Munich, 1966, e.g. on pages 121 to 205.

A characteristic value range of 100 to 300, preferably 100 to 130, is generally worked with according to the invention.

For the manufacture of the foam the foaming can also be carried out in closed moulds according to the invention. For this the reaction mixture is introduced into a mould. Metal, e.g. aluminium, or plastics material, e.g. epoxy resin, is considered as mould material.

In the mould the foamable reaction mixture foams up and forms the moulding. The mould foaming can be carried out in such a way that the moulded part has a cellular structure on its surface. It can however also be carried out in such a way that the moulded part has a compact skin and a cellular core. According to the invention it is possible to proceed in this connection in such a way that an amount of foamable reaction mixture is introduced into the mould such that the foam formed just fills the mould. It is also possible to work, however, so that more foamable reaction mixture is introduced into the mould than is necessary for filling the mould interior with foam. In the last-mentioned case "overcharging" is therefore practised; such a method of operation is known e.g. from U.S. Pat. Nos. 3,178,490 and 3,182,104.

Use is often also made for the mould foaming of "outer mould release agents" known per se, such as silicone oils. So-called "inner mould release agents" can however also be used, optionally in a mixture with outer mould release agents, such as have become known e.g. from DE-OS 2 121 670 and 2 307 589.

Chilling and refrigerating units are preferably foamed out according to the invention.

Foams can naturally, however, also be manufactured by slabstock foaming or by the continuous laminator method known per se.

The rigid foams obtainable according to the invention are furthermore used e.g. in the building trade and for the lagging of district heating pipes and containers.

EMBODIMENTS I. Manufacture of o-Toluene Diamine (TDA)/Propylene Oxide Polyethers Example A

19.6 kg of o-TDA, the mixture of 2,3- and 3,4-TDA obtained as by-product during the manufacture of TDA, are placed in a 100 l reactor suitable for reactions with alkylene oxides and 27.9 kg of propylene oxide (3 mol/mol TDA) are added within 2 hours after thorough washing with nitrogen at 110.degree. to 125.degree. C. and 2 to 3 bar nitrogen. After 2 hours subsequent reaction and the addition of 600 g of 45% aqueous potassium hydroxide solution, 42.5 kg of propylene oxide are then incorporated. After a subsequent reaction time of 4 hours at 110.degree. to 125.degree. C. the alkaline polyether is neutralized with lactic acid. After the addition of 90 g of Ionol, small amounts of readily volatile components are removed under vacuum. 90 kg of a polyether with the following analytical data are obtained:

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     OH number (ESA)    403                                                    

     OH number (PSA)    362                                                    

     .eta.              31320 mPa .multidot. s/25.degree. C.                   

     ______________________________________
Example B

The same amounts of TDA and propylene oxide are used as in Example A. In contrast to Example A, however, the preparation is catalyzed with only 400 g of 45% aqueous potassium hydroxide solution. The preparation is neutralized with acetic acid. After working up, 90 kg of a polyether with the following analytical data are obtained:

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     LeA 30 832                                                                

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     OH number (ESA)    389                                                    

     OH number (PSA)    356                                                    

     .eta.              36690 mPa .multidot. s/25.degree. C.                   

     ______________________________________
Example C (Comparison)

19.6 kg of o-TDA are placed in a 100 l reactor and 32.6 kg of propylene oxide (3.5 mol/mol TDA) are added within 2.5 hours after thorough washing with nitrogen at 110.degree. to 125.degree. C. and 2 to 3 bar nitrogen. After 2 hours subsequent reaction and the addition of 400 g of 45% aqueous potassium hydroxide solution, 37.8 kg of propylene oxide are then incorporated. After a subsequent reaction time of 4 hours at 110.degree. to 125.degree. C. the alkaline polyether is neutralized with lactic acid. After the addition of 90 g of Ionol, small amounts of readily volatile components are removed under vacuum. A polyether with the following analytical data is obtained:

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     OH number (ESA)    398                                                    

     OH number (PSA)    380                                                    

     .eta.              48750 mPa .multidot. s/25.degree. C.                   

     ______________________________________

The OH values given have been determined both by the acetic anhydride (ESA) method and by the phthalic acid (PSA) method. The difference in the values of the two methods gives the content in secondary NH groups.

II. Manufacture of Rigid PUR Foams

(PW=parts by weight)

Example 1

Polyol component:

Mixture of

60 parts by wt of a polyether polyol according to the invention with OH number (ESA) 403, manufactured by the polyaddition of 1,2-propylene oxide to o-toluene diamine according to Example A,

30 parts by wt of a polyether polyol with hydroxyl number (ESA) 450, manufactured by the polyaddition of 1.2-propylene oxide to a mixture of sucrose and ethylene glycol,

10 parts by wt of a phthalic acid/diethylene glycol ester ether with hydroxyl number (ESA) 300,

2 parts by wt of water,

2 parts by wt of a foam stabilizer on silicone base (Tegostab.RTM. B 8443),

1.2 parts by wt of N,N-dimethylcyclohexylamine.

The polyol component dissolves 40 parts by wt of cyclopentane or >40 parts by wt of 1,1,1,4,4,4-hexafluorobutane.

The polyol component has a viscosity of 2500 mPa.s at 25.degree. C.

The core polyol has a calculated functionality of 3.4.

Isocyanate component:

Polymeric MDI (crude MDI), NCO content 31.5 wt %.

Manufacture of a rigid PUR foam:

100 parts by wt of the polyol component and 13 parts by wt of cyclopentane are mixed by means of a laboratory stirrer (1000 rpm) at 20.degree. C. 113 parts by wt of this mixture are then stirred with 130 parts by wt of the isocyanate component. A defined amount of the reaction mixture is poured into a mould with the dimensions 22.times.22.times.6 cm and foamed up into a compressed rigid foam slab. Several of these mouldings are manufactured and demoulded after different times. When the moulding has cooled, its irreversible swelling is determined.

Example 2 (Comparative Example)

Polyol component:

Mixture of

60 parts by wt of a polyether polyol with OH number (ESA) 400, manufactured by polyaddition of 1,2-propylene oxide to sucrose

30 parts by wt of a polyether polyol with hydroxyl number (ESA) 450, manufactured by the polyaddition of 1.2-propylene oxide to a mixture of sucrose and ethylene glycol,

10 parts by wt of a phthalic acid-diethylene glycol ester ether with hydroxyl number (ESA) 300,

2 parts by wt of water,

2 parts by wt of a foam stabilizer on silicone base (Tegostab.RTM. B 8443),

2.6 parts by wt of N,N-dimethylcyclohexylamine.

The polyol component dissolves 11 parts by wt of cyclopentane or 7 parts by wt of 1,1,1,4,4,4-hexafluoro-butane.

The polyol component has a viscosity of 2200 mpa.s at 25.degree. C.

The core polyol has a calculated functionality of 3.8.

Tests with i-pentane or n-pentane as blowing agent did not produce a satisfactory solubility in the polyol component.

Isocyanate component:

Polymeric MDI (crude MDI), NCO content 31.5 wt %.

Manufacture of a rigid PUR foam:

100 parts by wt of the polyol component and 13 parts by wt of cyclopentane are mixed by means of a laboratory stirrer (1000 rpm) at 20.degree. C. 113 parts by wt of this mixture are then stirred with 130 parts by wt of the isocyanate component. A defined amount of the reaction mixture is poured into a mould with the dimensions 22.times.22.times.6 cm and foamed up into a compressed rigid foam slab. Several of these mouldings are manufactured and demoulded after different times. When the moulding has cooled, its irreversible swelling is determined.

Example 3 (Comparative Example)

Polyol component:

Mixture of

60 parts by wt of a polyether polyol with OH number (ESA) 400, manufactured by the polyaddition of 1,2-propylene oxide to trimethylolpropane,

30 parts by wt of a polyether polyol with hydroxyl number (ESA) 450, manufactured by the polyaddition of 1.2-propylene oxide to a mixture of sucrose and ethylene glycol,

10 parts by wt of a phthalic acid-diethylene glycol ester ether with hydroxyl number (ESA) 300,

2 parts by wt of water,

2 parts by wt of a foam stabilizer on silicone base (Tegostab.RTM. B 8443),

2.6 parts by wt of N,N-dimethylcyclohexylamine.

The polyol component dissolves 29 parts by wt of cyclopentane, or 18 parts by wt of 1,1,1,4,4,4-hexafluoro-butane.

The polyol component has a viscosity of 500 mpa.s at 25.degree. C.

The core polyol has a calculated functionality of 2.8.

Tests with i-pentane and n-pentane as blowing agent did not produce a satisfactory solubility in the polyol component.

Isocyanate component:

Polymeric MDI (crude MDI), NCO content 31.5 wt %.

Manufacture of a rigid PUR foam:

100 parts by wt of the polyol component and 13 parts by wt of cyclopentane are mixed by means of a laboratory stirrer (1000 rpm) at 20.degree. C. 113 parts by wt of this mixture are then stirred with 130 parts by wt of the isocyanate component. A defined amount of the reaction mixture is poured into a mould with the dimensions 22.times.22.times.6 cm and foamed up into a compressed rigid foam slab. Several of these mouldings are manufactured and demoulded after different times. When the moulding has cooled, its irreversible swelling is determined.

The results of the mould retention time measurement for Examples 1 to 3 showed the following:

Whereas only small swell values were obtained for the formulation of Example 1 based on the o-toluene diamine-propylene oxide polyether according to the invention, the formulations of Examples 2 and 3 show far higher swell values.

Claims

1. A polyether polyol containing tertiary amino groups and having an OH number of from about 300 to about 500 produced by adding only propylene oxide to o-toluene diamine produced by

a) reacting 3 mol of propylene oxide with o-toluene diamine,
b) adding an alkali catalyst to the reaction mixture of a), and
c) adding propylene oxide to the reaction mixture of b) until a product having an OH number of from about 300 to about 500 is obtained.

2. The polyol of claim 1 having an OH number of from about 350 to about 420.

3. A process for the production of a polyether polyol comprising:

a) reacting 3 mol of propylene oxide with o-toluene diamine,
b) adding an alkali catalyst to the reaction mixture of a), and
c) adding propylene oxide to the reaction mixture of b) until a product having an OH number of from 300 to 500 is obtained.

4. The process of claim 3 in which propylene oxide is added in step c) until the OH number is from 350 to 420.

5. A polyol formulation useful for the production of rigid polyurethane foams comprising a mixture containing from 40 to 80% by weight of the polyether polyol of claim 1.

6. The polyol formulation of claim 5 which further includes a sucrose-based polyether polyol having an OH number of from about 350 to about 500.

7. The polyol formulation of claim 6 which further includes a phthalic acid ester polyol.

8. The polyol formulation of claim 7 in which cyclopentane is present as a blowing agent.

9. The polyol formulation of claim 7 in which n-pentane and/or isopentane is present as a blowing agent.

10. The polyol formulation of claim 7 in which a hydrofluoroalkane is present as a blowing agent.

11. The polyol formulation of claim 7 in which 1,1,1,4,4,4-hexafluorobutane and/or 1,1,1,3,3-pentafluoropropane is present as a blowing agent.

12. The polyol formulation of claim 7 in which a blowing agent selected from the group consisting of cyclopentane, n-pentane, isopentane, 1,1,1,4,4,4-hexafluorobutane, 1,1,1,3,3-pentafluoropropane and mixtures thereof is present.

13. The polyol formulation of claim 5 in which cyclopentane is present as a blowing agent.

14. The polyol formulation of claim 5 in which n-pentane and/or isopentane is present as a blowing agent.

15. The polyol formulation of claim 5 in which a hydrofluoroalkane is present as a blowing agent.

16. The polyol formulation of claim 5 in which 1,1,1,4,4,4-hexafluorobutane and/or 1,1,1,3,3-pentafluoropropane is present as a blowing agent.

17. The polyol formulation of claim 5 in which a blowing agent selected from the group consisting of cyclopentane, n-pentane, isopentane, 1,1,1,4,4,4-hexafluorobutane, 1,1,1,3,3-pentafluoropropane and mixtures thereof is present.

18. A process for the production of a rigid polyurethane foam comprising reacting

a) an organic polyisocyanate with
b) the polyol formulation of claim 12, optionally in the presence of
c) an isocyanate-reactive compound containing at least two isocyanate-reactive hydrogen atoms,
d) water, or
e) a blowing agent which is not present in the polyol formulation b) and which is not water.

19. A process for the production of a rigid polyurethane foam comprising reacting

a) an organic polyisocyanate with
b) the polyol formulation of claim 17, optionally in the presence of
c) an isocyanate-reactive compound containing at least two isocyanate-reactive hydrogen atoms,
d) water, or
e) a blowing agent which is not present in the polyol formulation b) and which is not water.
Referenced Cited
U.S. Patent Documents
RE33290 August 7, 1990 Naka et al.
4562290 December 31, 1985 Korczak et al.
4904707 February 27, 1990 Lunney
4970018 November 13, 1990 Lunney
5260347 November 9, 1993 Krueger et al.
5461084 October 24, 1995 Doerge
5583197 December 10, 1996 Harrison et al.
Foreign Patent Documents
293060 November 1988 EPX
0374628 June 1990 EPX
0495134 July 1992 EPX
495134 July 1992 EPX
Patent History
Patent number: 5840781
Type: Grant
Filed: Jul 15, 1997
Date of Patent: Nov 24, 1998
Assignee: Bayer Aktiengesellschaft (Leverkusen)
Inventors: Karl-Werner Dietrich (Odenthal), Manfred Dietrich (Leverkusen), Wilhelm Lamberts (Sao Paulo-SP), Walter Klan (Leverkusen)
Primary Examiner: Rachel Gorr
Attorneys: Joseph C. Gil, Lyndanne M. Whalen
Application Number: 8/875,805